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Metabolic response to different glycemic indexes of pre-exercise meal

Resposta metabólica a diferentes índices glicêmicos da refeição pré-exercício

Respuesta metabólica a diferentes índices glucémicos de la ingestión de alimentos antes de los ejercicios

Abstracts

INTRODUCTION:

To ensure performance and health, the type of food and the time of pre-exercise ingestion should be considered by practitioners of morning physical activity. Objective: This study assessed the metabolic response after pre-exercise meals with different glycemic indexes (GI) and in the fasting state adopting different types of hydration.

METHODS:

Twelve men performed four experimental tests; two with pre-exercise meals of high GI (HGI) and low GI (LGI), and two were performed in the fasting state with hydration: water (H2O) and carbohydrate drink (CHO). Each test consisted of a pre-exercise rest period of 30 minutes followed by 60 minutes of cycle ergometer with continuous load equivalent to 60% of the extrapolated maximal oxygen consumption (VO2MaxExt). During the exercise, participants were hydrated every 15 minutes with 3mL per kg body weight. During each experimental test, venous blood samples were obtained for fasting and at 15-minute intervals during rest, and every 20 minutes during exercise. The gas analysis was carried out in periods of 5 minutes every 20 minutes of exercise.

RESULTS:

There was no difference in substrate oxidation. After 20 minutes of exercise, pre-exercise food intake procedures showed similar behavior, having only reduced blood glucose levels compared to fasting procedures (p<0.01). There was maintenance of blood glucose at stable and higher levels during exercise in relation to the other tests in the fast procedure with CHO.

CONCLUSION:

The data suggest that despite the similar metabolic behavior between LGI and HGI meals, the adoption of a LGI meal before the morning exercise seems to be a more suitable feeding practice due to higher tendency of rebound hypoglycemia after HGI meal and when morning exercise is performed on fasting, hydration with CHO seems to minimize the hypoglycemic risk arising from that state.

carbohydrates; breakfast; fasting; energy drinks; blood glucose


INTRODUÇÃO:

Para garantir o desempenho e a saúde, o tipo de alimento e o tempo de ingestão pré-exercício devem ser considerados pelos praticantes de atividade física matutina. Objetivo: Este estudo avaliou a resposta metabólica após as refeições pré-exercício com diferentes índices glicêmicos (IG) e no estado de jejum, adotando diferentes tipos de hidratação.

MÉTODOS:

Doze homens realizaram quatro testes; dois com refeições pré-exercício de alto IG (AIG) e baixo IG (BIG), e dois foram conduzidos em jejum com hidratação: água (H2O) e bebida carboidratada (CHO). Cada teste consistiu em 30 minutos de repouso antes do exercício, seguidos por 60 minutos de bicicleta ergométrica com carga contínua equivalente a 60% do consumo máximo de oxigênio extrapolado (VO2MaxExt). Durante o exercício, os participantes foram hidratados a cada 15 minutos com 3 ml por kg de peso corporal. Durante cada teste, foram obtidas amostras de sangue venoso em jejum e em intervalos de 15 minutos durante o repouso, e a cada 20 minutos durante o exercício. A análise de gases foi realizada em períodos de 5 minutos a cada 20 minutos de exercício.

RESULTADOS:

Não houve diferença na oxidação de substrato. Depois de 20 minutos de exercício, os procedimentos de ingestão de alimentos pré-exercício apresentaram comportamento semelhante, mostrando somente redução dos níveis de glicemia em comparação com os procedimentos em jejum (p < 0,01). Houve manutenção da glicemia em níveis estáveis e mais altos durante o exercício com relação aos outros testes no procedimento de jejum com CHO.

CONCLUSÃO:

Os dados sugerem que, apesar do comportamento metabólico semelhante entre refeições de BIG e AIG, a adoção de uma refeição de BIG antes do exercício matinal parece ser uma prática de alimentação mais adequada devido à maior propensão de hipoglicemia de rebote após a refeição AIG e, quando o exercício matinal é realizado em jejum, a hidratação com CHO parece minimizar o risco hipoglicêmico decorrente desse estado.

carboidratos; desjejum; jejum; bebidas energéticas; glicemia


INTRODUCCIÓN:

Para garantizar el desempeño y la salud, deben ser considerados por los practicantes de actividad física matutina el tipo de alimento y el tiempo de ingestión antes de los ejercicios. Objetivo: Este estudio evaluó la respuesta metabólica después de la ingestión de alimentos antes de los ejercicios con diferentes índices glucémicos (IG) y en estado de ayuno, adoptando diferentes tipos de hidratación.

MÉTODOS:

Doce hombres realizaron cuatro tests; dos con alimentación antes de los ejercicios de alto IG (AIG) y bajo IG (BIG), y dos fueron conducidos en ayunas con hidratación: agua (H2O) y bebida carbohidratada (CHO). Cada test consistió en 30 minutos de reposo antes de los ejercicios, seguidos por 60 minutos de bicicleta ergométrica con carga continua equivalente a 60% del consumo máximo de oxígeno extrapolado (VO2MaxExt). Durante los ejercicios, los participantes fueron hidratados a cada 15 minutos con 3 ml por kg de peso corporal. Durante cada test, fueron obtenidas muestras de sangre venosa en ayunas y en intervalos de 15 minutos durante el reposo, y a cada 20 minutos durante los ejercicios. El análisis de gases fue realizado en períodos de 5 minutos a cada 20 minutos de ejercicio.

RESULTADOS:

No hubo diferencia en la oxidación de sustrato. Después de 20 minutos de ejercicios, los procedimientos de ingestión de alimentos antes de los ejercicios presentaron comportamiento semejante, mostrando solamente reducción de los niveles de glucemia en comparación con los procedimientos en ayunas (p < 0,01). Hubo mantenimiento de la glucemia en niveles estables y más altos durante los ejercicios con relación a los otros tests en el procedimiento de ayunas con CHO.

CONCLUSIÓN:

Los datos sugieren que, a pesar del comportamiento metabólico semejante entre comidas de BIG y AIG, la adopción de una comida de BIG antes de los ejercicios matinales parece ser una práctica de alimentación más adecuada debido a la mayor propensión de hipoglucemia de rebote después de la comida AIG y, cuando los ejercicios matinales son realizados en ayunas, la hidratación con CHO parece minimizar el riesgo hipoglucémico proveniente de ese estado.

carbohidratos; desayuno; ayuno; bebidas energéticas; glucemia


INTRODUCTION

The glycemic index (GI) of food reflects its absorption rate and subsequent glycemic response, which may occur more quickly and at higher levels in the case of high glycemic index (HGI > 70), or more slowly and at lower levels in the case of low glycemic index (LGI < 55)1Jeukendrup AE, Killer SC. The myths surrounding pre-exercise carbohydrate feeding. Ann Nutr Metab. 2010;57(Suppl 2):18-25..

This functional tool has been widely used to determine the most suitable pre-exercise meal for the maintenance of blood glucose levels during physical exercise1Jeukendrup AE, Killer SC. The myths surrounding pre-exercise carbohydrate feeding. Ann Nutr Metab. 2010;57(Suppl 2):18-25., avoiding the occurrence of hypoglycemia (blood glucose < 70 mg / dL)2Standards of medical care in diabetes--2015: summary of revisions. Diabetes Care. 2015;38(1):S1-S94.. Special attention is devoted to the performance of morning physical activity because due to climatic conditions and labor activities, it is a time of great preference by the population, and it is the time of day in which the individual's muscle and liver glycogen reserves are depleted due to the overnight fasting period3McArdle WD, Katch FI, Katch LF. Fisiologia do exercício: energia, nutrição e desempenho humano. 7a ed. Rio de Janeiro: Guanabara Koogan; 2011..

In this context, it is known that in practical terms, the time prior to physical activity for food intake is restricted4Brasil TA, Pinto JA, Cocate PG, Chácara RP, Marins JCB. Avaliação do hábito alimentar de praticantes de atividade física matinal. Fit Perf J. 2009;8(3):153-63., and breakfast can lead to rebound hypoglycemia5Coyle EF, Coggan AR, Hemmert MK, Lowe RC, Walters TJ. Substrate usage during prolonged exercise following a preexercise meal. J Appl Physiol (1985). 1985;59(2):429-33. , which occurs due to high glucose uptake by the muscle, caused by the action of high insulin levels, which also inhibits lipolysis, added to the muscular action itself1Jeukendrup AE, Killer SC. The myths surrounding pre-exercise carbohydrate feeding. Ann Nutr Metab. 2010;57(Suppl 2):18-25.. This condition obviously impairs an ideal performance during exercise, and should then be avoided. Moreover, training performed in total fasting state can also accelerate the onset of a hypoglycemia condition during exercise, which is also harmful.

In the case of training performed in total fasting state is important to consider a hydration with carbohydrate drink as a strategy to maintain normoglycemic values, however the studies are limited to evaluating it in relation to performance6Del Coso J, Muñoz-Fernández VE, Muñoz G, Fernández-Elías VE, Ortega JF, Hamouti N, et al. Effects of a caffeine-containing energy drink on simulated soccer performance. PLoS One. 2012;7(2):e31380. . Moreover, according to a systematic review7Faria VC, Oliveira GA, Sales SS, Marins JCB, Lima LM. Índice glicêmico da refeição pré-exercício e metabolismo da glicose na atividade aeróbica. Rev Bras Med Esporte. 2014;20(2):156-60. conducted previously there are no studies that evaluate the metabolic impact of a meal offered 30 minutes prior to exercise.

Thus, given that hypoglycemia levels are related to sickness, nausea, malaise, and in some extreme cases, with fainting, harming not only the quality of the activity, but exposing the organism to a risk condition8Nybo L, Møller K, Pedersen BK, Nielsen B, Secher NH. Association between fatigue and failure to preserve cerebral energy turnover during prolonged exercise. Acta Physiol Scand. 2003;179(1):67-74. , the aim of this study was to evaluate the metabolic response after pre-exercise meals with different glycemic indexes and in fasting state adopting different types of hydration.

METHODS

Twelve healthy and physically active men (age 22.9 ± 2 years, body weight 74 ± 5.5 kg, VO2max 42.2 ± 8.9 ml.kg-1.min-1) voluntarily participated in this study. The experimental procedure was approved by the Research Ethics Committee (REC) of the institution with process number 140/2011 and all participants signed the Informed Consent Form (ICF) endorsed by the REC. The following inclusion criteria were considered: the regular performance of physical activities, absence of cardiovascular risk factors and any chronic degenerative disease.

Initially, participants completed the Informed Consent Form, the PAR-Q questionnaire9Pollock ML, Wilmore JH. Exercício na saúde e na doença: avaliação e prescrição para prevenção e reabilitação. 2a ed. Rio de Janeiro: Guanabara Koogan; 1993., a medical history, and were submitted to clinical and anthropometric evaluations (Biodynamics Model 310e, Seattle, WA, USA), and to submaximal test to determine the workload.

To determine the workload, a metabolic gas analyzer (VO-2000, Aerosport, Medgraphics, St. Paul, Minnesota) was used during test in electromagnetic cycle ergometer (SciFit model ISO1000, Oklahoma, United States) with load increment up to 85% of the MHRcalculated, which was obtained by the equation THRtraining heart rate = % (HRmax - HRrest) + HRrest 1010 Karvonen MJ, Kentala E, Mustala O. The effects of training on heart rate; a longitudinal study. Ann Med Exp Biol Fenn. 1957;35(3):307-15. , in which HRmax was calculated by the equation MHRcalculated = 202 - 0.72 (age)1111 Jones NL, Makrides L, Hitchcock C, Chypchar T, McCartney N. Normal standards for an incremental progressive cycle ergometer test. Am Rev Respir Dis. 1985;131(5):700-8. . This test started with a 3-minute warm-up exercise with load corresponding to the body weight of each volunteer, and from this load, 30 W were added every minute until reaching the target HR. With the aim of preserving the volunteer's physical integrity and according with Marsh (2012)1212 Marsh CE. Evaluation of the American College of Sports Medicine submaximal treadmill running test for predicting VO2max. J Strength Cond Res. 2012;26(2):548-54. , extrapolated VO2max(VO2MaxEx) was adopted to calculate the workload, as it was obtained from equation generated by a linear regression with HR and O2 consumption values recorded during exercise up to the time it was stopped (85% of the MHRcalculated), and from it, the load corresponding to 60% of the VO2MaxEx was determined.

The subjects were instructed to make a similar diet between tests and avoiding exercising on the test day.

Two dietary procedures according to the GI of meals were adopted, with nutritional composition detailed in table 1. Meals were LGI and HGI, both with hydration with water during exercise.

Table 1.
Nutrition Composition of pre-exercise meals.

The GI of meals was calculated by the method of Wolever and Jenkins1313 Wolever TM, Jenkins DJ. The use of the glycemic index in predicting the blood glucose response to mixed meals. Am J Clin Nutr. 1986;43(1):167-72. with GI values taken from the International table of GI1414 Foster-Powell K, Holt SH, Brand-Miller JC. International table of glycemic index and glycemic load values: 2002. Am J Clin Nutr. 2002;76(1):5-56. , and in the absence of the exact food, the value of the food that most resembled was used.

Besides these procedures, two other procedures in the fasting state were also performed and are differentiated by the type of hydration: water or carbohydrate drink (CHO).

A standardized procedure was adopted for all experimental tests (figure 1), which was composed of a 5-minute warm-up exercise in cycle ergometer with progressive load from 45 to 55% of the VO2MaxExt, performed after a rest period prior to exercise of 30 minutes, followed by 60 minutes of cycle ergometer with continuous load equivalent to 60% of the VO2MaxExt. During exercise, participants hydrated every 15 minutes with 3 ml per kg body weight.

Figure 1.
Schematic representation of experimental procedures.

During each experimental test, fasting blood samples and in 15-minute intervals during rest and every 20 minutes during exercise were obtained. The equipment used was i-StatOne Blood Analyzer (i-Stat(r) Abbott, Illinois, USA) with cartridge CG8, obtaining blood samples by venipuncture in one of the forearm superficial veins with placement of scalp and collection of 1 ml of blood in each sampling time. Analyses of blood glucose, hematocrit, hemoglobin, calcium, sodium and potassium were performed. In addition, gas analysis was performed (VO-2000, Aerosport, Medgraphics, St. Paul, Minnesota) in periods of 5 minutes every 20 minutes of exercise.

To evaluate the fluid balance, body weight and urine density were recorded before and after exercise and urine volume was recorded after exercise, and weight loss was calculated (initial weight - final weight)1515 Osterberg KL, Pallardy SE, Johnson RJ, Horswill CA. Carbohydrate exerts a mild influence on fluid retention following exercise-induced dehydration. J Appl Physiol (1985). 2010;108(2):245-50. .

For statistical analysis were used the analysis of variance (ANOVA) and the paired t-test. The significance level adopted was 5% and the Sigma Stat software version 1.0 was used.

RESULTS

There was no significant difference in mean respiratory quotient (RQ) between procedures throughout exercise, as well as the oxidation values ​​of CHO and fat (table 2).

Table 2.
Respiratory quotient (RQ), CHO oxidation and fat oxidation in different periods during exercise.

There was a glycemic peak in the rest period 15 min after the ingestion of HGI and LGI meals in relation to fasting procedures (p <0.01), but not significantly different from one another. After 20 minutes of exercise, pre-exercise food intake procedures kept a similar behavior, only showing reduced blood glucose levels compared to the other procedures (p <0.01). At 40 and 60 minutes of exercise, fasting with H2O showed glucose concentration lower than that of fasting with CHO (p = 0.015). The glycemic response during the four procedures is shown in figure 2.

Figure 2.
Blood glucose concentration (mg/dL) during rest and exercise in the four procedures. ap<0.01: HGI and LGI vs. fasting procedures. bp = 0.015: fasting with CHO vs. fasting with H2O.

The hemoglobin and hematocrit concentrations showed no significant differences between procedures at all evaluation times; however, in all tests, exercise caused an increase in these variables in relation to rest (table 3).

Table 3.
Hematocrit and hemoglobin levels during rest and exercise.

There were differences between groups regarding potassium concentration at 60 minutes of exercise, being higher in LGI procedure in relation to fasting with CHO (p = 0.019) (figure 3C). Calcium concentrations remained constant throughout the testing period in all procedures (figure 3A); however, sodium and potassium levels increased after the onset of exercise, and at the end of exercise, sodium levels returned to resting values, while potassium values remained high throughout the exercise (figure 3B and 3C).

Figure 3.
Total blood calcium (mmol/L), sodium and potassium concentrations (mEq/L) during rest and exercise in the four procedures. C: * p = 0.019: LGI vs. fasting with CHO.

Among the parameters related to fluid balance only the final urine volume differed between groups, being higher in HGI compared to fasting with H2O (p = 0.041). Moreover, there was a significant difference (p = 0.007) between initial and final urine density in the HGI procedure (table 4).

Table 4.
Hydration parameters.

DISCUSSION

HGI foods stimulate greater and faster insulinemic and glycemic response, the latter actually occurred in this study (figure 2). This behavior has been associated with increased absorption of available glucose, which is enhanced during physical exercise, since there is translocation of the glucose transporter protein (GLUT-4) to the surface of the muscle fibers caused by its contractions1Jeukendrup AE, Killer SC. The myths surrounding pre-exercise carbohydrate feeding. Ann Nutr Metab. 2010;57(Suppl 2):18-25..

High insulin levels can inhibit lipolysis, making the energy consumption increasingly dependent on CHO oxidation1616 Karamanolis IA, Laparidis KS, Volaklis KA, Douda HT, Tokmakidis SP. The effects of pre-exercise glycemic index food on running capacity. Int J Sports Med. 2011;32(9):666-71. . In the present study, regardless of dietary intake of HGI or LGI or fasting state with hydration with H2O or CHO-electrolyte drink, no difference was observed in CHO and fat oxidation during exercise, which is consistent with result of the study by Moore et al. 1717 Moore LJ, Midgley AW, Thomas G, Thurlow S, McNaughton LR. The effects of low-and high-glycemic index meals on time trial performance. Int J Sports Physiol Perform. 2009;4(3):331-44. , who compared HGI and LGI, and with results obtained by Chen et al. 1818 Chen YJ, Wong SH, Chan CO, Wong CK, Lam CW, Siu PM. Effects of glycemic index meal and CHO-electrolyte drink on cytokine response and run performance in endurance athletes. J Sci Med Sport. 2009;12(6):697-703. and Wong et al. 1919 , Wong SH Chan OW, Chen YJ, Hu HL, Lam CW, Chung PK. Effect of preexercise glycemic-index meal on running when CHO-electrolyte solution is consumed during exercise. Int J Sport Nutr Exerc Metab. 2009;19(3):222-42. , who assessed pre-exercise meals with different GI but with hydration during exercise with CHO-electrolyte drink. The current results can be justified by the presence of fructose in the LGI meal composition, since the metabolism of fructose in the liver occurs from the second glycolysis reaction, being readily oxidized2020 Lê KA, Tappy L. Metabolic effects of fructose. Curr Opin Clin Nutr Metab Care. 2006;9(4):469-75. and thus showing a behavior similar to HGI meal, as evidenced by the study of Sun et al. 2121 Sun FH, Wong SH, Huang YJ, Chen YJ, Tsang KF. Substrate utilization during brisk walking is affected by glycemic index and fructose content of a pre-exercise meal. Eur J Appl Physiol. 2012;112(7):2565-74..

In the postprandial glycemic response, there was a peak 15 minutes after ingestion of both meals, with significant differences in relation to fasting procedures, but unlike the vast majority of studies1616 Karamanolis IA, Laparidis KS, Volaklis KA, Douda HT, Tokmakidis SP. The effects of pre-exercise glycemic index food on running capacity. Int J Sports Med. 2011;32(9):666-71. , 1818 Chen YJ, Wong SH, Chan CO, Wong CK, Lam CW, Siu PM. Effects of glycemic index meal and CHO-electrolyte drink on cytokine response and run performance in endurance athletes. J Sci Med Sport. 2009;12(6):697-703. , 1919 , Wong SH Chan OW, Chen YJ, Hu HL, Lam CW, Chung PK. Effect of preexercise glycemic-index meal on running when CHO-electrolyte solution is consumed during exercise. Int J Sport Nutr Exerc Metab. 2009;19(3):222-42. , it showed no difference between pre-exercise HGI and LGI meals (figure 2).

Although with no significant differences, pre-exercise HGI meal showed higher glycemic elevation in relation to LGI meal at 15 postprandial minutes and at 30 minutes, immediately before the onset of exercise, blood glucose levels in LGI procedure had already reached baseline while those of HGI procedure still showed higher values ​​(figure 2). These results may have a clinical implication, since blood glucose and insulin levels are higher in response to HGI meal, and if exercise starts with levels still high, there may be a rapid decrease in blood glucose levels in the first moments of exercise, usually at 15 minutes1Jeukendrup AE, Killer SC. The myths surrounding pre-exercise carbohydrate feeding. Ann Nutr Metab. 2010;57(Suppl 2):18-25., which is a phenomenon called rebound hypoglycemia or reactive hypoglycemia5Coyle EF, Coggan AR, Hemmert MK, Lowe RC, Walters TJ. Substrate usage during prolonged exercise following a preexercise meal. J Appl Physiol (1985). 1985;59(2):429-33. .

The decrease in plasma glucose levels actually occurred at 20 minutes of exercise (figure 2), but with both pre-exercise meals, HGI and LGI; however, the mean values ​​remained within the normoglycemic range (70 to 99 mg / dL)2Standards of medical care in diabetes--2015: summary of revisions. Diabetes Care. 2015;38(1):S1-S94.. Nevertheless, it is noteworthy that the intensity adopted in this study was low, 60% of the VO2MaxEx, and that values ​​below 70 mg / dL could be achieved during high-intensity exercise.

Considering the report of Jeukendrup and Killer1Jeukendrup AE, Killer SC. The myths surrounding pre-exercise carbohydrate feeding. Ann Nutr Metab. 2010;57(Suppl 2):18-25. in which some individuals are more likely to develop hypoglycemia, it could be observed that in both HGI as LGI pre-exercise meal at 20 minutes of exercise, 33.3% of volunteers had glucose values ​​below 70 mg / dL, and from these, only one showed the same hypoglycemic values ​​in both meals, and only one volunteer, when submitted to HGI procedure, dropped out due to hypoglycemia symptoms previously mentioned8Nybo L, Møller K, Pedersen BK, Nielsen B, Secher NH. Association between fatigue and failure to preserve cerebral energy turnover during prolonged exercise. Acta Physiol Scand. 2003;179(1):67-74. . These results point out to the need for monitoring the individual impact of pre-exercise diet, especially in athletes submitted to systematic training, since individual characteristics may or may not facilitate a condition of rebound hypoglycemia.

From 20 minutes and throughout the exercise, fasting with CHO obtained glucose values ​​similar to those of HGI and LGI procedures, which agrees with the results of Chen et al. 1818 Chen YJ, Wong SH, Chan CO, Wong CK, Lam CW, Siu PM. Effects of glycemic index meal and CHO-electrolyte drink on cytokine response and run performance in endurance athletes. J Sci Med Sport. 2009;12(6):697-703. and Wong et al.1919 , Wong SH Chan OW, Chen YJ, Hu HL, Lam CW, Chung PK. Effect of preexercise glycemic-index meal on running when CHO-electrolyte solution is consumed during exercise. Int J Sport Nutr Exerc Metab. 2009;19(3):222-42. , who showed that the CHO consumption during exercise minimizes the metabolic difference arising from GI.

The data obtained in this study demonstrated that the risks in performing exercises in the fasting state can be minimized by hydration with CHO, when significantly higher blood glucose values compared to ​​fasting with H2O at 40 and 60 minutes of exercise are observed (figure 2). It was also observed that at 60 minutes of exercise, only in fasting with H2O procedure, blood glucose levels below 70 mg / dL were recorded, and that this showed a tendency to decrease, which would allow a higher occurrence of hypoglycemic values in case exercise is prolonged. This behavior was also observed in a previous study2222 , Faria VC Cazal MM, Cabral CAC,. Marins JCB Influência do índice glicêmico na glicemia em exercício físico aeróbico. Motriz. 2011;17(3):395-405.; however, no significant difference was observed between fasting procedures.

The results of the fluid balance (table 4) showed greater final urine volume (p = 0.041) in the HGI procedure, which is consistent with the fact that the final urine density was significantly lower (p=0.007) compared to the initial volume in the same procedure. That was the only fluid change observed, which does not prevent us from concluding that the type of hydration adopted in experimental tests (3 ml/kg body weight) was sufficient to maintain the initial state of volunteers, since there was no significant body weight loss after exercise. However, in all procedures, participants were hypo-hydrated to begin the exercise (urine density > 1.020 g.ml-1), according to Casa et al. 2323 Casa DJ, Armstrong LE, Hillman SK, Montain SJ, Reiff RV, Rich BS, et al. National athletic trainers' association position statement: fluid replacement for athletes. J Athl Train. 2000;35(2):212-24..

Hydration was also sufficient to maintain hematocrit (40 to 54%) and hemoglobin values (13.5 to 18 g / dL) at normal levels for men2424 Fischbach FT, Dunning MB. A manual of laboratory and diagnostic tests. 9th ed. Philadelphia: Lippincott; 2014. (table 3); however, exercise duration and intensity adopted in this experiment provided hemoconcentration during exercise, which warns us about the importance of adequate hydration especially during physical activities longer and more intense than usual, considering that individuals begin their physical practice dehydrated, as observed in the present study and reported by other authors2525 , Marins JCB Ferreira FG. Nível de conhecimento dos atletas universitários da UFV sobre hidratação. Fit Perf J. 2005;4(3):175-87. , 2626 Peacock OJ, Stokes K, Thompson D. Initial hydration status, fluid balance, and psychological affect during recreational exercise in adults. J Sports Sci. 2011;29(9):897-904..

A progressive dehydration condition will cause a decrease in plasma volume during the exercise, leading to cardiovascular adaptation by increasing the heart rate in an attempt to maintaining sufficient cardiac output to meet the active muscles and assist in the thermoregulatory mechanism, since the venous return and consequently the systolic volume are affected2727 Carvalho T, Mara LS. Hidratação e nutrição no esporte. Rev Bras Med Esporte. 2010;16(2):144-8.. In certain extreme dehydration conditions, the cardiovascular adaptation can trigger a collapse, producing a cardiac arrest2828 Somboonwong J, Sanguanrungsirikul S, Pitayanon C. Heat illness surveillance in schoolboys participating in physical education class in tropical climate: an analytical prospective descriptive study. BMJ Open. 2012;2(4). pii: e000741. doi: 10.1136/bmjopen-2011-000741.
https://doi.org/10.1136/bmjopen-2011-000...
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Of ions evaluated, only sodium maintained throughout the exercise within normal values (135 to 145 mEq / L)2929 Scott MG, LeGrys VA, Klutts JS. Electrolytes and blood gases. In: Burtis CA, Ashwood ER, Bruns DE, editors. Fundamentals of clinical chemistry and molecular diagnostics (Tietz). 7th ed. Philadelphia: Sauders Elsevier; 2014. p. 412-429., whereas ionic calcium (1.15 to 1.33 mmol / L)29 29 Scott MG, LeGrys VA, Klutts JS. Electrolytes and blood gases. In: Burtis CA, Ashwood ER, Bruns DE, editors. Fundamentals of clinical chemistry and molecular diagnostics (Tietz). 7th ed. Philadelphia: Sauders Elsevier; 2014. p. 412-429.and potassium (3.5 to 5.0 mEq / L)29 showed values ​​above physiological limit. Although no significant difference was observed between the four procedures for the total calcium and sodium levels, significantly higher potassium levels were observed at the end of 60 minutes of exercise in the LGI procedure compared to fasting with CHO (figure 3C). This can be attributed to the lower stimulation of insulin release caused by LGI food in contrast to stimulation every 15 minutes caused by CHO, as hypoinsulinemia can be considered as a possible cause of hyperpotassemia3030 Vieira Neto OM, Moyses Neto M. Distúrbios do equilíbrio hidroeletrolítico. Medicina, Ribeirão Preto. 2003;36:325-37., or due to the total composition of potassium in the LIG meal be greater when compared to HIG meal (964 mg vs. 599 mg).

The elevation of potassium levels at the beginning of exercise in all procedures occurs because during physical activity, it is released from the intracellular medium to the extracellular medium of the muscle tissue and then into the bloodstream, and as this tissue is the largest potassium deposit in the body3030 Vieira Neto OM, Moyses Neto M. Distúrbios do equilíbrio hidroeletrolítico. Medicina, Ribeirão Preto. 2003;36:325-37., changes caused by exercise are highlighted.

CONCLUSION

Despite the similar metabolic behavior between LGI and HGI meals, the adoption of LGI meal before morning exercise appears to be the most suitable nutritional strategy due to the greater propensity of rebound hypoglycemia after HGI meal. When performed in fasting, hydration with CHO seems to minimize the hypoglycemic risk arising from this state. However, although the insulinemic response has not been analyzed, further studies are needed to assess the potassium behavior during exercise after LGI meal.

REFERENCES

  • 1
    Jeukendrup AE, Killer SC. The myths surrounding pre-exercise carbohydrate feeding. Ann Nutr Metab. 2010;57(Suppl 2):18-25.
  • 2
    Standards of medical care in diabetes--2015: summary of revisions. Diabetes Care. 2015;38(1):S1-S94.
  • 3
    McArdle WD, Katch FI, Katch LF. Fisiologia do exercício: energia, nutrição e desempenho humano. 7a ed. Rio de Janeiro: Guanabara Koogan; 2011.
  • 4
    Brasil TA, Pinto JA, Cocate PG, Chácara RP, Marins JCB. Avaliação do hábito alimentar de praticantes de atividade física matinal. Fit Perf J. 2009;8(3):153-63.
  • 5
    Coyle EF, Coggan AR, Hemmert MK, Lowe RC, Walters TJ. Substrate usage during prolonged exercise following a preexercise meal. J Appl Physiol (1985). 1985;59(2):429-33.
  • 6
    Del Coso J, Muñoz-Fernández VE, Muñoz G, Fernández-Elías VE, Ortega JF, Hamouti N, et al. Effects of a caffeine-containing energy drink on simulated soccer performance. PLoS One. 2012;7(2):e31380.
  • 7
    Faria VC, Oliveira GA, Sales SS, Marins JCB, Lima LM. Índice glicêmico da refeição pré-exercício e metabolismo da glicose na atividade aeróbica. Rev Bras Med Esporte. 2014;20(2):156-60.
  • 8
    Nybo L, Møller K, Pedersen BK, Nielsen B, Secher NH. Association between fatigue and failure to preserve cerebral energy turnover during prolonged exercise. Acta Physiol Scand. 2003;179(1):67-74.
  • 9
    Pollock ML, Wilmore JH. Exercício na saúde e na doença: avaliação e prescrição para prevenção e reabilitação. 2a ed. Rio de Janeiro: Guanabara Koogan; 1993.
  • 10
    Karvonen MJ, Kentala E, Mustala O. The effects of training on heart rate; a longitudinal study. Ann Med Exp Biol Fenn. 1957;35(3):307-15.
  • 11
    Jones NL, Makrides L, Hitchcock C, Chypchar T, McCartney N. Normal standards for an incremental progressive cycle ergometer test. Am Rev Respir Dis. 1985;131(5):700-8.
  • 12
    Marsh CE. Evaluation of the American College of Sports Medicine submaximal treadmill running test for predicting VO2max. J Strength Cond Res. 2012;26(2):548-54.
  • 13
    Wolever TM, Jenkins DJ. The use of the glycemic index in predicting the blood glucose response to mixed meals. Am J Clin Nutr. 1986;43(1):167-72.
  • 14
    Foster-Powell K, Holt SH, Brand-Miller JC. International table of glycemic index and glycemic load values: 2002. Am J Clin Nutr. 2002;76(1):5-56.
  • 15
    Osterberg KL, Pallardy SE, Johnson RJ, Horswill CA. Carbohydrate exerts a mild influence on fluid retention following exercise-induced dehydration. J Appl Physiol (1985). 2010;108(2):245-50.
  • 16
    Karamanolis IA, Laparidis KS, Volaklis KA, Douda HT, Tokmakidis SP. The effects of pre-exercise glycemic index food on running capacity. Int J Sports Med. 2011;32(9):666-71.
  • 17
    Moore LJ, Midgley AW, Thomas G, Thurlow S, McNaughton LR. The effects of low-and high-glycemic index meals on time trial performance. Int J Sports Physiol Perform. 2009;4(3):331-44.
  • 18
    Chen YJ, Wong SH, Chan CO, Wong CK, Lam CW, Siu PM. Effects of glycemic index meal and CHO-electrolyte drink on cytokine response and run performance in endurance athletes. J Sci Med Sport. 2009;12(6):697-703.
  • 19
    , Wong SH Chan OW, Chen YJ, Hu HL, Lam CW, Chung PK. Effect of preexercise glycemic-index meal on running when CHO-electrolyte solution is consumed during exercise. Int J Sport Nutr Exerc Metab. 2009;19(3):222-42.
  • 20
    Lê KA, Tappy L. Metabolic effects of fructose. Curr Opin Clin Nutr Metab Care. 2006;9(4):469-75.
  • 21
    Sun FH, Wong SH, Huang YJ, Chen YJ, Tsang KF. Substrate utilization during brisk walking is affected by glycemic index and fructose content of a pre-exercise meal. Eur J Appl Physiol. 2012;112(7):2565-74.
  • 22
    , Faria VC Cazal MM, Cabral CAC,. Marins JCB Influência do índice glicêmico na glicemia em exercício físico aeróbico. Motriz. 2011;17(3):395-405.
  • 23
    Casa DJ, Armstrong LE, Hillman SK, Montain SJ, Reiff RV, Rich BS, et al. National athletic trainers' association position statement: fluid replacement for athletes. J Athl Train. 2000;35(2):212-24.
  • 24
    Fischbach FT, Dunning MB. A manual of laboratory and diagnostic tests. 9th ed. Philadelphia: Lippincott; 2014.
  • 25
    , Marins JCB Ferreira FG. Nível de conhecimento dos atletas universitários da UFV sobre hidratação. Fit Perf J. 2005;4(3):175-87.
  • 26
    Peacock OJ, Stokes K, Thompson D. Initial hydration status, fluid balance, and psychological affect during recreational exercise in adults. J Sports Sci. 2011;29(9):897-904.
  • 27
    Carvalho T, Mara LS. Hidratação e nutrição no esporte. Rev Bras Med Esporte. 2010;16(2):144-8.
  • 28
    Somboonwong J, Sanguanrungsirikul S, Pitayanon C. Heat illness surveillance in schoolboys participating in physical education class in tropical climate: an analytical prospective descriptive study. BMJ Open. 2012;2(4). pii: e000741. doi: 10.1136/bmjopen-2011-000741.
    » https://doi.org/10.1136/bmjopen-2011-000741
  • 29
    Scott MG, LeGrys VA, Klutts JS. Electrolytes and blood gases. In: Burtis CA, Ashwood ER, Bruns DE, editors. Fundamentals of clinical chemistry and molecular diagnostics (Tietz). 7th ed. Philadelphia: Sauders Elsevier; 2014. p. 412-429.
  • 30
    Vieira Neto OM, Moyses Neto M. Distúrbios do equilíbrio hidroeletrolítico. Medicina, Ribeirão Preto. 2003;36:325-37.

Publication Dates

  • Publication in this collection
    Jul-Aug 2015

History

  • Received
    29 Mar 2015
  • Accepted
    22 June 2015
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